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Heroin Dependence clinical trials

View clinical trials related to Heroin Dependence.

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NCT ID: NCT01471145 Completed - Clinical trials for Opioid-Related Disorders

Depot Naltrexone Mechanism of Action in Heroin Dependent Patients Using fMRI and SPECT

XRNT
Start date: January 2013
Phase: Phase 4
Study type: Interventional

The aim of this project is to study brain functions of 20 heroin addicts (compared to brain functions of 20 healthy controls) just before and during a three month extended release naltrexone treatment using functional MRI and dopamine transporter SPECT. The following hypotheses are tested: - XRNT modulates the fMRI response to drug cues in predetermined brain regions. - The expression of striatal transporters (assessed with SPECT) will decrease after a three-month course of extended release naltrexone

NCT ID: NCT01457872 Completed - Clinical trials for Substance Use Disorders

Malmö Treatment Referral and Intervention Study

MATRIS
Start date: October 2011
Phase: N/A
Study type: Interventional

This study aims to study and implement active referral of heroin users from a syringe exchange programme to evidence-based treatment for heroin addiction. Patients are randomized to either a strength-based case management intervention or a control group, while both groups receive referral to medical investigation for inclusion in substitution treatment for heroin addiction. The hypothesis is that syringe exchange can be used for referral to effective treatment, and that a strength-based intervention can increase the number of patients who are successfully referred and enter treatment.

NCT ID: NCT01447212 Completed - Opioid Dependence Clinical Trials

Study to Assess Longer-term Opioid Medication Effectiveness (SALOME)

SALOME
Start date: December 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study, SALOME, is to determine if 1) the closely supervised provision of injectable, hydromorphone (HDM; trade name Dilaudidā„¢) is as effective as injectable diacetylmorphine (DAM; heroin) in the treatment of chronic, multi-morbid opioid-dependent individuals who have not benefited sufficiently from conventional treatments, and if a switch to the oral equivalent of hydromorphone and diacetylmorphine is as effective as the injection form. The availability of an effective, licensed opioid medication such as hydromorphone, for substitution treatment of chronic, multi-morbid treatment-refractory opioid-dependent individuals, would be of immense impact locally and internationally. It could help to establish alternative treatment options where for non-medical reasons Heroin Assisted Treatment would not be acceptable. Thus, one result could be the expansion of treatment options for the most difficult to treat heroin dependent persons. This would also be an important step for secondary prevention of HIV and Hepatitis C as well as a better integration of those patients in other medical treatments. Switching from intravenous to oral application would also reduce a lot of potential risk factors (like overdose, seizures, infections, etc) and side effects associated with the injection route. Additionally it could make these treatments more feasible in normal treatment settings, like existing methadone services.

NCT ID: NCT01395797 Terminated - Nicotine Dependence Clinical Trials

Pioglitazone for Heroin and for Nicotine Dependence

Start date: March 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of the proposed research is to improve the effectiveness of treatments for opioid and for nicotine dependence by testing a novel pharmacological strategy. Specifically, pioglitazone, a peroxisome proliferator-activated gamma receptor (PPARĪ³) agonist, will be used as an adjunct to agonist-based treatment.

NCT ID: NCT01315184 Completed - Clinical trials for Opioid-Related Disorders

Study of Computer-Based Treatment for Drug Dependence

RLSS
Start date: July 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the whether an automated telephone-based system is useful and helpful for opioid dependent patients receiving buprenorphine in primary care. The Recovery Line support system is a Therapeutic Interactive Voice Response system based on cognitive behavioral therapy (CBT). The Recovery Line support system includes a variety of modules presenting the basic principles and strategies of CBT. Each module includes learning sections and activities sections to provide direct guidance in using skills. The Recovery Line support system is interactive and also includes a questionnaire to help patients identify problems and recommend modules for use, as well as an inspiration section, an introduction, and an immediate assistance menu. Following development of an initial system the current trial will recruit 40 patients receiving buprenorphine maintenance from a physician provider in the local community. Patients will be randomly (flip of a coin) to receive the Recover Line Support system or to treatment as usual with their physician. Patients assigned to TIVR will be trained on the system and provided 24-hr access to the TIVR system for a four week period. Primary outcome variables will be how long patients remain in treatment, self-reported abstinence from opioids and other drugs, and abstinence as measured by weekly drug screens. It is expected that patients assigned to TIVR will better treatment outcomes than patients assigned to TAU.

NCT ID: NCT01144390 Active, not recruiting - Heroin Dependence Clinical Trials

Effect Study of Optimized Intervention to Heroin Addicts

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to explore barriers and determine whether optimizing protocol is effective in the treatment of heroin dependence in community-based MMT clinics.

NCT ID: NCT01093248 Recruiting - Heroin Addiction Clinical Trials

Methadone Maintenance Treatment Outcome Study in Taiwan

M0508
Start date: July 2009
Phase: N/A
Study type: Observational

Opioid abuse is a complex problem, which not only impacts on the affected individuals' physical and psychological health, but also threatens public security and the productivity of the society. Further, through needle sharing and sexual contacts, injecting drug users (IDUs) have become laden with HIV and HIV related health problems, representing a serious public health threat all over the world. In Taiwan, since the identification of the first HIV-infected IDU in 1987, the incident cases have continued to increase, reaching a height of 2,461 in 2005. In order to contain the epidemics of HIV among IDUs, and to prevent its spread to the population in general, the Center for Disease Control (CDC) collaborated with the Department of Justice to initiate and implement a number of harm reduction programs in 2005. The fact that opioid addiction is officially treated as a health rather than a legal issue itself represents a remarkable milestone in Taiwan. Among these harm reduction programs, including needle and syringe exchange for IDUs as well as substitution treatment approaches for opioid dependence, methadone maintenance treatment (MMT) perhaps represents the most most important and most crucial component. Remarkably, in a relatively short time span, more than 60 MMT programs were established, which enrolled more than 15,000 heroin addicts. This notwithstanding, the overall and differential effectiveness of these MMT service delivery systems, as well as the characteristics of these programs and the patients that might contribute toward treatment response or failure remain largely unknown. Such knowledge base is crucial for establishing standardized and feasible outcome evaluation processes for opioid addicts receiving MMT programs, as well as for the further improvement of the efficacy and effectiveness of these programs, in Taiwan. In order to address some of these issues, this study adopts a multi-site, prospective clinical follow-up design. It aims at establishing a research network for examining MMT outcome, developing standardized MMT outcome assessment instruments and procedures, and identifying predictors of MMT outcome. The findings may contribute to the better understanding of the characteristics of opioid addicts, the effectiveness of MMT and remaining service needs for opioid addicts in Taiwan.

NCT ID: NCT00894452 Completed - Heroin Dependence Clinical Trials

Variance of Oral Methadone Dosage: Description of Implicated Factors

METHADOSE
Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this study is to describe clinical, pharmacokinetic and genetic factors associated with the variance of oral methadone dosage for patients at the steady state of heroin dependence maintenance treatment. The hypothesis is that the investigators can predict 70% of the variance with few factors, including CYP 3A4 function measured with oral midazolam challenge.

NCT ID: NCT00759005 Completed - Heroin Dependence Clinical Trials

Effect of Stress on Heroin-Related Memory Retrieval

Start date: March 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether cortisol and propranolol are effective in the modulation of stress induced heroin-related retrieval enhancement.

NCT ID: NCT00750217 Unknown status - Heroin Addiction Clinical Trials

Transfer From Methadone to Buprenorphine Maintenance Treatment Using Buprenorphine Patches

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Buprenorphine is an important alternative to methadone in the maintenance treatment of heroin addiction. Transfer from methadone to buprenorphine requires a reduction of daily methadone dosage below 30 mg to avoid withdrawal after the first buprenorphine intake. The study hypothesis states that the transfer from a daily methadone dosage between 60 mg and 100 mg to buprenorphine can be carried out without withdrawal using buprenorphine patches (35 micro grams per hour) within 12 to 48 hours after last methadone intake.